United States · FDA National Drug Code directory
Midazolam in Sodium Chloride
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 25021-688_44922f28-68c0-45c6-ad4c-0cc7706a78b4
- Product NDC
- 25021-688
- Form
- INJECTION, SOLUTION
- Composition / generic term
- Midazolam Hydrochloride
- Labeler
- Sagent Pharmaceuticals
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20250415
- Source listing expiry
- 20261231
Source-listed ingredients
- MIDAZOLAM HYDROCHLORIDE — 1 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 10 BAG in 1 CARTON (25021-688-82) / 50 mL in 1 BAG · 25021-688-82
- 20 BAG in 1 CARTON (25021-688-87) / 100 mL in 1 BAG · 25021-688-87
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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